A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383699



Internal ID21041252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119233849..119330597hg38UCSC Ensembl
chr4:120155004..120251752hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3896749
hg1996749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211976
Samples
Known GenesC4orf3, FABP2, USP53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383699
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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